CLASS I Food recall · Reported 28 May 2014 · FDA Enforcement Report
Blue Bunny Premium Ice Cream, Bordeaux Cherry Chocolate recalled
Wells Enterprises is recalling Blue Bunny Premium Ice Cream, Bordeaux Cherry Chocolate, distributed in Iowa, Indiana, Kansas. The recall was initiated on 2 May 2014 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1961-2014
- FDA event ID
- 68198
- Recalling firm
- Wells Enterprises, Le Mars, IA
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 2 May 2014
- FDA classified
- 22 May 2014
- Reported
- 28 May 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Egg
- Product category
- Ice Cream & Frozen Desserts
Timeline
| 2 May 2014 | Recall initiated by company | |
| 22 May 2014 | Classified by FDA | +20 days |
| 28 May 2014 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The product may contain egg which is not listed on the ingredient label.
Product as listed by the FDA
Blue Bunny Premium Ice Cream, Bordeaux Cherry Chocolate, 1.75 quart. Packaged in 4/56-oz carton cases. Item # 745152, UPC 070640034123. Manufactured by Wells Enterprises, Inc., Le Mars, IA.
Where it was distributed
The product was distributed to KS, IN and IA.
Questions about this recall
Why was it recalled?
The product may contain egg which is not listed on the ingredient label.
Which lots are affected?
Lot 40010 TTT 19115 4100, Best Used by 10/9/15
Where was it sold?
The product was distributed to KS, IN and IA.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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